Home About us Editorial board Ahead of print Current issue Search Archives Submit article Instructions Subscribe Contact Us Login 
An Official Publication of the Indian Association of Oral and Maxillofacial Pathologists


 
  Table of Contents    
ORIGINAL ARTICLE  
Year : 2018  |  Volume : 22  |  Issue : 3  |  Page : 341-346
 

Estimation of salivary Candida albicans counts in asthmatic adult patients taking anti-asthmatic medication for 3–5 years


1 Independent Researcher, Mysuru, Karnataka, India
2 Department of Oral Pathology and Microbiology, College of Dental Sciences, Davangere, Karnataka, India
3 Department of Oral Pathology, Dental College, Regional Institute of Medical Science, Imphal, Manipur, India
4 Department of Pulmonary Medicine, JJM Medical College and Hospital, Davangere, Karnataka, India

Date of Submission20-Feb-2017
Date of Acceptance15-Jun-2018
Date of Web Publication14-Dec-2018

Correspondence Address:
Kumari Alka
Independent Researcher, Mysuru, Karnataka
India
Login to access the Email id

Source of Support: None, Conflict of Interest: None


DOI: 10.4103/jomfp.JOMFP_36_17

Rights and Permissions

 

   Abstract 


Background: Bronchial asthma is a chronic inflammatory disease of airways. The disease itself along with the principal medication used makes the oral cavity susceptible to most common opportunistic infection, i.e., oral candidiasis. There are many species of Candida causing oral candidiasis, but the most prevalent among them is Candida albicans. Hence, assessing C. albicans count in response to disease and its treatment is necessary. This enables us to educate asthma patients about side effects of medication and highlight the necessity for oral health care, thereby improving their quality of life.
Aims: The present study aims to evaluate the effects of asthma and its medication on C. albicans count in saliva samples of asthmatic adult patients taking medication for 3–5 years and compare C. albicans count in saliva samples among cases and controls.
Materials and Methods: Thirty asthmatic adults taking medication for asthma since 3–5 years' age ranging from 20 to 50 years and equal number of age- and sex-matched healthy participants were included in the study. In both groups, saliva was collected and inoculated on Sabouraud Dextrose Agar culture plates for estimation of C. albicans counts. C. albicans counts were assessed in colony-forming unit/milliliter.
Statistical Analysis: Mann–Whitney U-test and Fisher's exact t-test were used.
Results: The C. albicans count is significantly higher among asthmatics than healthy individuals.
Conclusions: The present study concludes that there is increased candidal growth among asthmatics as compared to their normal healthy counterpart.


Keywords: Asthma, Candida albicans, colony-forming units, corticosteroids, saliva, β2-agonist


How to cite this article:
Alka K, Amberkar VS, Mohan Kumar K P, Nandini D B, Vidyasagar B. Estimation of salivary Candida albicans counts in asthmatic adult patients taking anti-asthmatic medication for 3–5 years. J Oral Maxillofac Pathol 2018;22:341-6

How to cite this URL:
Alka K, Amberkar VS, Mohan Kumar K P, Nandini D B, Vidyasagar B. Estimation of salivary Candida albicans counts in asthmatic adult patients taking anti-asthmatic medication for 3–5 years. J Oral Maxillofac Pathol [serial online] 2018 [cited 2019 Jun 16];22:341-6. Available from: http://www.jomfp.in/text.asp?2018/22/3/341/247391





   Introduction Top


Bronchial asthma is a chronic disorder characterized by airway inflammation, reversible airway obstruction and airway hyperresponsiveness.[1] Asthma is one of the most common diseases in industrialized countries, and there is convincing evidence, suggesting that its prevalence and morbidity are increasing despite better recognition.[2] This disease is characterized by increased responsiveness of airway to nonspecific stimuli, leading to symptoms such as wheezing, coughing, chest tightness and dyspnea.[3] Asthma is a growing public health problem affecting over 300 million people worldwide including almost all age groups.[4] Bronchial asthma is a common disease in India with a prevalence rate of about 1696 women and 1627 men per 100000 people in 2010 and is increasing.[5],[6],[7]

Apart from the morbidity caused by the disease per se, medication to prevent or treat asthma has more adverse effects on various body systems along with oral cavity.[8] The principle medication used in asthma is bronchodilators and β2-agonists and inhalational therapy is the major way of drug delivery system in asthmatics.[4] Only 10%–20% of the dose from an inhaler reaches the lung and rest remains in the oral pharyngeal region. These remnant corticosteroids are exposed to oral tissues for the prolonged period of time, due to which oral defense system is suppressed.[10] Prolonged use of β2-agonists is associated with diminished salivary production and secretion; in severe cases, it can lead to xerostomia, which alters the oral cavity environment.[11],[12],[13] Therefore, combined effect of these principal used medications in asthmatics reduces the local immunity and makes the oral cavity susceptible to opportunistic infections such as oral candidiasis.[14]

Oral candidiasis is by far the most common oral opportunistic infection in man.[15] The Candida genus is comprised over 150 species of asporogenous “yeast-like” fungi.[16] The majority of Candida species are unable to grow at 37°C and are, therefore, not normally associated with human colonization.[17],[18],[19] However, several species do persist as commensal microorganisms within humans in about 2%–70% of the general population and figures do vary depending on the population examined.[20],[21] There are many species of Candida, but the most prevalent one which is recovered from the oral cavity, in both commensal state and in cases of oral candidiasis, is Candida albicans and it accounts for over 80% of all oral yeast isolates.[16],[22] Common oral Candida species isolated from oral cavity are C. albicans, Candida glabrata, Candida guilliermondii, Candida krusei, Candida parapsilosis, Candida pseudotropicalis and Candida stellatoidea; these can act as opportunistic pathogens in immunocompromised host. A change from the harmless commensal existence of Candida to a pathogenic state can also occur following alteration of the oral cavity environment to one that favors the growth of Candida. The causes of such changes are the so-called predisposing factors for candidal infection (candidiasis) and most often these relate to a weakening of host immune defense.[23] The ability of Candida to convert from commensals to pathogenic from is attributed to its multiple virulence factors.[24]

Oral candidal colonization and candidiasis have recently received increased attention by the health-care providers and researchers alike, particularly following the widespread use of broad-spectrum antibiotics and immunosuppressant therapy in various diseases.[25] One of the common of such diseases is asthma, where inhalation therapy leads to local immunosuppression, leading to candidiasis, which can also precipitate asthmatic attack.[26]

Thus, evaluating the candidal superinfection in response to asthma and its treatment is necessary, to improve its management and improve the quality of life of asthmatics.


   Materials and Methods Top


Institutional ethical clearance was obtained and the present study was conducted in the Department of Oral Pathology and Microbiology, College of Dental Sciences, Davangere, along with the Department of Pulmonary Medicine, JJM Medical College and Hospital, Davangere.

A total of 60 participants comprising 30 asthmatics and 30 age- and sex-matched healthy controls were included in the study [Table 1] after obtaining an informed consent and a detailed case history. The mean age of the study participants was 34.23 years, and there were 22 females and 8 males in each group.
Table 1: Inclusion and exclusion criteria for cases and controls

Click here to view


Sample collection

All the appointments for sample collection were given between 9.00 am to 11.00 am. Participants were informed not to eat prior giving sample. Before sample collection, participants were asked to rinse the mouth and sit upright and to swallow existing saliva. After a minimum of 5-min rest, unstimulated whole saliva was collected by asking the participants to spit the whole saliva into sterile container for 5–10 min, and samples were then carried immediately in a vaccine carrier with ice pack to the laboratory for further processing. The sample was immediately inoculated.

Microbial procedure

After serial dilution of saliva sample, a standard dilution was taken and 50 μl of that standard dilution inoculated onto already prepared Sabouraud Dextrose Agar (SDA) culture medium using lawn culture method. One area of the culture plate was marked and known candidal organisms were inoculated [Figure 1]. The plates were incubated at 37° C for 24–48 h aerobically. After incubations, Candida colonies were examined morphologically, and germ tube test was done for confirmation of C. albicans. Colony counting was done using digital colony counter.
Figure 1: Colonies of Candida on Sabouraud Dextrose Agar with positive control

Click here to view


Statistical analysis

Obtained data were entered in Microsoft Excel and analyzed using SPSS version 21 (IBM Corp. Armork, NY: IBM Corp) using Mann–Whitney U-test, Chi-square test and Fisher's exact test.


   Results Top


In the present study, the cases with colony-forming unit (CFU)/ml <400 were considered as the carriers of Candida and >400 were considered as pathogenic.[27],[28]

Assessment of salivary Candida albicans counts in colony-forming unit/milliliter in study groups

Among cases, 22 individuals showed candidal growth and 8 individuals did not show any candidal growth. Among controls, none of the individuals showed candidal growth [Table 2].
Table 2: Assessment of salivary Candida albicans counts in colony-forming unit/ml in study groups

Click here to view


Assessment of salivary Candida albicans counts in colony-forming unit/milliliter among cases

There were 12 individuals in ≤400 CFU/ml group, and there were 18 individuals in ≥401 CFU/ml group. The median of ≤400 CFU/ml group was 0.00 and ≥401 CFU/ml group was 2600. There was a statistically significant difference between both the groups with regard to CFU/ml (P = 0.00) [Table 3].
Table 3: Assessment of salivary Candida albicans counts in colony-forming unit/ml among cases

Click here to view


Intergroup comparison of salivary Candida albicans counts in median colony-forming unit/milliliter between asthmatics and controls

There was a statistically significant difference between cases and controls with regard to CFU/ml (P = 0.00) [Table 4].
Table 4: Intergroup comparison of salivary Candida albicans counts in median colony-forming unit/ml between asthmatics and controls

Click here to view


Association of duration of disease with salivary Candida albicans counts in colony-forming unit/milliliter

For analysis, purpose duration of asthma was divided into 3, 4 and 5 years. Eleven (36.4%) were taking medication for 3 years, 11 (36.6%) were taking medication for 4 years and 8 (26.6%) were taking medication for 5 years. There was no significant association between duration of disease and CFU/ml of C. albicans counts (P = 0.06) [Table 5].
Table 5: Association of duration of disease with salivary Candida albicans counts in colony-forming unit/ml

Click here to view


Association of doses of anti-asthmatic medication with salivary Candida albicans counts in colony-forming unit/milliliter

In the present study, patients were taking anti-asthmatic medication in the dose of 100 or 250 or 500 mg. There was no statistically significant association between doses of anti-asthmatic medication and CFU/ml of C. albicans counts (P = 0.13) [Table 6].
Table 6: Association of doses of anti-asthmatic medication with salivary Candida albicans counts in colony-forming unit/ml

Click here to view


Association of severity of the disease with salivary Candida albicans counts in colony-forming unit/milliliter

In the present study, patients were having mild or moderate or severe disease. There was no statistically significant association of severity of the disease with C. albicans counts in CFU/ml (P = 0.23) [Table 7].
Table 7: Association of severity of the disease with salivary Candida albicans count in colony-forming unit/ml

Click here to view



   Discussion Top


Bronchial asthma is chronic debilitating disease, the effects of which are not always restricted to the pathogenesis and disease per se but also to the standard treatment protocol followed.[7] Pathogenesis involves genetically susceptible individuals on exposure to stimulus, or allergens show increased responsiveness leading to a hyperinflammatory reaction in the airway mucous membrane leading to a plethora of symptoms.[29] The treatment targets hyperresponsive inflammatory system using anti-inflammatory medication to avoid generalized immune suppressed state for prolong period of duration and local delivery is preferred, directly through nebulization. Any drug which is nebulized or inhaled will have their residual presence in the oronasal region for prolong duration.[30] Thus; the oral environment is susceptible to alteration due to nebulized drug usage. As in asthma, the various drugs used alter or suppress the immune system and are delivered by nebulization bringing them in contact with the oral cavity for a prolonged period of time which can lead to alteration in oral bioflora and facilitate the growth of opportunistic infections.[26]

With this background, our study was designed to estimate the prevalence of C. albicans, most common opportunistic organism in adult asthmatics, wherein nebulization is the choice of drug delivery and compares the CFU of C. albicans with age- and sex-matched controls.

To estimate the set objectives, 30 individuals diagnosed with asthma under medication who fulfilled the criteria previously mentioned and their age- and sex-matched healthy individuals were included in this study as cases and controls, respectively. CFU/ml of C. albicans of saliva was estimated among the cases and controls using standard methods on SDA. Among 30 cases, 22 (73.3%) of the individuals showed candidal growth and 8 (26%) showed no candidal growth, indicating that compared to healthy individual asthmatics under medication showed microfloral alteration facilitating candidal growth.

Among the asthmatics, the salivary C. albicans CFU/ml was analyzed and the median value obtained was 1000, and a statistically significant difference was demonstrated between two groups, i.e., cases and controls. Further among asthmatics with candidal growth, individuals having salivary Candida count in CFU/ml ≥401 were 18 and ≤401 were 12 (CFU/ml ≥401 was considered as pathogenic).[27],[28]

All the above findings indicate that there is increased an incidence of C. albicans among asthmatics using anti-asthmatic medications such as corticosteroids and β2-agonists. It was also noted that asthmatics showed CFU count similar to that of infective candidiasis, i.e., ≥401 CFU/ml of saliva.

Among above-mentioned results, it was noteworthy that although CFU counts were high and indicate candidal infection, none of the cases were symptomatic for oral candidiasis. This possibly suggests that the infection was subclinical or a microbiotic change, facilitating increased candidal growth without producing symptoms.

Numerous similar studies indicate and support the above-mentioned facts that there is increased candidal infectability among asthmatics using inhaled anti-asthmatic medication.[14],[31],[32],[33],[34] Various concepts for this finding have been explained which include an interplay between disease, medication and host.[16]

  • Bronchial asthma facilitating candidal growth – Restricted salivary flow in asthmatics makes them susceptible to mouth breathing. Mouth breathing on a long duration induces xerostomia and an altered microbial environment of oral cavity both of which facilitate candidal adhesion and colonization among asthmatics
  • Host factor affected by anti-asthmatic medication leading to increased candidal growth – Asthmatic condition control is gained by medication which falls mainly under two categories, β2-agonists which promote bronchial relaxation and corticosteroids which suppress the immune system.


Apart from the effects which ease the asthmatic condition, these drugs affect various systems and induce a favorable environment for candidal growth

  1. β2-agonists decreases the salivary flow which, in turns, leads to decreased salivary pH and also decreased biological active components such as amylase, salivary IgA, lysozyme and lactoferrin which favor the candidal growth
  2. Corticosteroids suppress the immune system and induced alterations facilitate growth by the following mechanisms:


    1. Neutrophils are the first line of defense and it kills 20%–30% of Candida regardless of the number of Candida in the oral cavity. This activity is diminished in asthmatics due to suppressed immunity
    2. Intracellular killing of Candida by myeloperoxidase-hydrogen peroxide-halide system is greatly reduced due to immune suppression caused by corticosteroids used by asthmatics
    3. Activation of T-cells produces a wide range of lymphokines that can, in turn, modulate the functions of macrophages and other leukocytes. Interferon-gamma is the only lymphokine known to increase the microbicidal activities of macrophages, which is reduced in asthmatics due to suppressed immunity.


The present study revealed no candidal carriage in healthy individuals on the contrary to the other reports. Cohen et al.[35] reported the prevalence of yeast as 35% in the oropharynx in healthy volunteers. Hanan et al.[36] in their study reported an incidence of 30%–45% of oral candidiasis in healthy adults. Zaremba et al.[37] conducted a study on the oral carriage of Candida in healthy individuals and reported a prevalence rate of 63.1%. Samaranayake found C. albicans in the oral cavity in about 3%–48% of healthy adults.[38]

This stark variation could possibly be attributed to other variables which are to be considered, such as geographical variations, nature and size of the sample selected and also the method of sample collection. Estimates of the prevalence of Candida species as human commensal vary considerably according to the size of the sample, type of person sampled and method of sampling adopted.[39],[40]

In the present study to eliminate the possible procedural error, a positive control was included in every culture plate. A colony of C. albicans stock culture confirmed by colony morphology on SDA and germ tube test was streaked in a corner along with the sample in the culture plate. In all the culture plates, the control streak produced candidal growth irrespective of sample yielding growth or not.

Among the asthmatics, the effect of duration of asthma, severity of disease and dosage of medication on salivary C. albicans count in CFU/ml was evaluated. There was no statistical evident association between the above parameters and C. albicans count. This suggests that the asthmatic individuals are prone to candidal carriage and/or infection irrespective of severity of disease, duration of disease or dosage of medication, and it is possible that they make the individual susceptible to candidal growth.

The exact effect of the above-mentioned parameters could not be evaluated from our study due to smaller sample and cross-sectional study design. A long-term follow-up study and larger sample can yield a clearer picture of the effect of the parameter on candidal susceptibility of asthmatics.

Hence, with our study, we could prove that there is an increased susceptibility of individuals with asthma to oral candidal growth. Although none of the asthmatic participants demonstrated clinically evident candidal lesion, candidal culture demonstrated levels of Candida equivalent to active candidal infection. These indicate oral environment in asthmatic facilitate candidal growth and colonization without any infection. Exact nature of change in the bacterial ecosystem, effects of the dose of medication, duration and severity of asthma needs further thorough evaluation.


   Conclusions Top


The present study concludes that there is increased candidal growth among asthmatics as compared to their normal healthy counterpart.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.



 
   References Top

1.
Shifren A, Witt C, Christie C, Castro M. Mechanisms of remodeling in asthmatic airways. J Allergy (Cairo) 2012;2012:316049.  Back to cited text no. 1
    
2.
Bitter E. Pulmonary Biology in Health and Disease. New York: Springer; 2002. p. 364.  Back to cited text no. 2
    
3.
Adkinson NF Jr., Bochner BS Jr., Burks AW, Busse WW, Holgate ST, Lemanske RF Jr., et.al. Middleton's Allergy: Principal and Practice. 8th ed. Philadelphia: Elsevier Health Sciences; 2013. p. 284-5.  Back to cited text no. 3
    
4.
Thomas MS, Parolia A, Kundabala M, Vikram M. Asthma and oral health: A review. Aust Dent J 2010;55:128-33.  Back to cited text no. 4
    
5.
Agarwal S. Asthma. In: South Asia Network for Chronic Disease. New Delhi; 2010. Available from: http://www.sancd.org/uploads/pdf/Asthma_factsheet.pdf. [Last accessed on 2011 Nov 17].  Back to cited text no. 5
    
6.
Salzman GA, Pyszczynski DR. Oropharyngeal candidiasis in patients treated with beclomethasone dipropionate delivered by metered-dose inhaler alone and with aerochamber. J Allergy Clin Immunol 1988;81:424-8.  Back to cited text no. 6
    
7.
Butler CC, Rollnick S, Kinnersley P, Jones A, Stott N. Reducing antibiotics for respiratory tract symptoms in primary care: Consolidating ‘why’ and considering ‘how’. Br J Gen Pract 1998;48:1865-70.  Back to cited text no. 7
    
8.
Ryberg M, Möller C, Ericson T. Effect of beta 2-adrenoceptor agonists on saliva proteins and dental caries in asthmatic children. J Dent Res 1987;66:1404-6.  Back to cited text no. 8
    
9.
Innes JA, Reid PT. Respiratory diseases. In: Boon NA, Colledge NR, Walker BR, Hunter JA, editors. Davidson's Principles and Practice of Medicine. 20th ed. Philadelphia: Churchill Livingstone, Elsevier; 2006. p. 670-8.  Back to cited text no. 9
    
10.
Tootla R, Toumba KJ, Duggal MS. An evaluation of the acidogenic potential of asthma inhalers. Arch Oral Biol 2004;49:275-83.  Back to cited text no. 10
    
11.
Holbrook WP, Kristinsson MJ, Gunnarsdóttir S, Briem B. Caries prevalence, Streptococcus mutans and sugar intake among 4-year-old urban children in Iceland. Community Dent Oral Epidemiol 1989;17:292-5.  Back to cited text no. 11
    
12.
Storhaug K. Caries experience in disabled pre-school children. Acta Odontol Scand 1985;43:241-8.  Back to cited text no. 12
    
13.
Maguire A, Rugg-Gunn AJ, Butler TJ. Dental health of children taking antimicrobial and non-antimicrobial liquid oral medication long-term. Caries Res 1996;30:16-21.  Back to cited text no. 13
    
14.
Ellepola AN, Samaranayake LP. Inhalational and topical steroids, and oral candidosis: A mini review. Oral Dis 2001;7:211-6.  Back to cited text no. 14
    
15.
Akpan A, Morgan R. Oral candidiasis. Postgrad Med J 2002;78:455-9.  Back to cited text no. 15
    
16.
Scully C, el-Kabir M, Samaranayake LP. Candida and oral candidosis: A review. Crit Rev Oral Biol Med 1994;5:125-57.  Back to cited text no. 16
    
17.
Brandão LR, Medeiros AO, Duarte MC, Barbosa AC, Rosa CA. Diversity and antifungal susceptibility of yeasts isolated by multiple-tube fermentation from three freshwater lakes in Brazil. J Water Health 2010;8:279-89.  Back to cited text no. 17
    
18.
Hsieh CW, Huang LY, Tschen EF, Chang CF, Lee CF. Five novel anamorphic, ascomycetous yeast species associated with mushrooms and soil. FEMS Yeast Res 2010;10:948-56.  Back to cited text no. 18
    
19.
Edelmann A, Krüger M, Schmid J. Genetic relationship between human and animal isolates of Candida albicans. J Clin Microbiol 2005;43:6164-6.  Back to cited text no. 19
    
20.
Darwazeh A, Darwazeh T. What makes oral candidiasis recurrent infection? A clinical view. J Mycol 2014;2014:1-5.  Back to cited text no. 20
    
21.
Williams DW, Kuriyama T, Silva S, Malic S, Lewis MA. Candida biofilms and oral candidosis: Treatment and prevention. Periodontol 2000 2011;55:250-65.  Back to cited text no. 21
    
22.
Pfaller MA, Diekema DJ. Epidemiology of invasive candidiasis: A persistent public health problem. Clin Microbiol Rev 2007;20:133-63.  Back to cited text no. 22
    
23.
Williams D, Lewis M. Pathogenesis and treatment of oral candidosis. J Oral Microbiol 2011;3:455-9.  Back to cited text no. 23
    
24.
Imron Nasution A. Virulence factors and pathogenicity of Candida albicans in oral candidiasis. World J Dent 2013;4:267-71.  Back to cited text no. 24
    
25.
Chopra S, Mahajan S, Mahajan G. Oral candidiasis: A review in HIV seropositive patients. CIBTech J Microbiol 2015;4:53-62.  Back to cited text no. 25
    
26.
Gumowski P, Lech B, Chaves I, Girard JP. Chronic asthma and rhinitis due to Candida albicans, Epidermophyton, and Trichophyton. Ann Allergy 1987;59:48-51.  Back to cited text no. 26
    
27.
Epstein JB, Pearsall NN, Truelove EL. Quantitative relationships between Candida albicans in saliva and the clinical status of human subjects. J Clin Microbiol 1980;12:475-6.  Back to cited text no. 27
    
28.
Balan P, B Gogineni S, Kumari NS, Shetty V, Lakshman Rangare A, L Castelino R, et al. Candida carriage rate and growth characteristics of saliva in diabetes mellitus patients: A Case-control study. J Dent Res Dent Clin Dent Prospects 2015;9:274-9.  Back to cited text no. 28
    
29.
Tippets B, Guilbert TW. Managing asthma in children, part 1: Making the diagnosis, assessing severity. Consult Pediatricians 2009;8:168-74.  Back to cited text no. 29
    
30.
Godara N, Godara R, Khullar M. Impact of inhalation therapy on oral health. Lung India 2011;28:272-5.  Back to cited text no. 30
  [Full text]  
31.
Fukushima C, Matsuse H, Tomari S, Obase Y, Miyazaki Y, Shimoda T, et al. Oral candidiasis associated with inhaled corticosteroid use: Comparison of fluticasone and beclomethasone. Ann Allergy Asthma Immunol 2003;90:646-51.  Back to cited text no. 31
    
32.
Mullaoglu S, Turktas H, Kokturk N, Tuncer C, Kalkanci A, Kustimur S, et al. Esophageal candidiasis and Candida colonization in asthma patients on inhaled steroids. Allergy Asthma Proc 2007;28:544-9.  Back to cited text no. 32
    
33.
Powell H, Gibson PG. Inhaled corticosteroid doses in asthma: An evidence-based approach. Med J Aust 2003;178:223-5.  Back to cited text no. 33
    
34.
Fukushima C, Matsuse H, Saeki S, Kawano T, Machida I, Kondo Y, et al. Salivary IgA and oral candidiasis in asthmatic patients treated with inhaled corticosteroid. J Asthma 2005;42:601-4.  Back to cited text no. 34
    
35.
Cohen R, Roth FJ, Delgado E, Ahearn DG, Kalser MH. Fungal flora of the normal human small and large intestine. N Engl J Med 1969;280:638-41.  Back to cited text no. 35
    
36.
Al-Abeid HM, Abu-Elteen KH, Elkarmi AZ, Hamad MA. Isolation and characterization of Candida spp. In Jordanian cancer patients: Prevalence, pathogenic determinants, and antifungal sensitivity. Jpn J Infect Dis 2004;57:279-84.  Back to cited text no. 36
    
37.
Zaremba ML, Daniluk T, Rozkiewicz D, Cylwik-Rokicka D, Kierklo A, Tokajuk G, et al. Incidence rate of Candida species in the oral cavity of middle-aged and elderly subjects. Adv Med Sci 2006;51 Suppl 1:233-6.  Back to cited text no. 37
    
38.
Samaranayake LP, MacFarlane TW. Hypothesis: On the role of dietary carbohydrates in the pathogenesis of oral candidosis. FEMS Microbiol Lett. 1985;27:1–5.  Back to cited text no. 38
    
39.
Dignani MC, Solomkin J, Anaisse EJ. Candida. In: Anaissie EJ, Mc Ginnis MR, Pfaller MA, editors. Textbook of Clinical Mycology. 1st ed. Ch. 8. Philadelphia: Churchill Livingstone; 2003. p. 195-239.  Back to cited text no. 39
    
40.
Kantheti LP, Reddy B, Ravikumar S, Anuradha CH, Chandrasekhar P, Rajeswari MR, et al. Isolation, identification, and carriage of Candida species in PHLAs and their correlation with immunological status in cases with and without HAART. J Oral Maxillofac Pathol 2012;16:38-44.  Back to cited text no. 40
  [Full text]  


    Figures

  [Figure 1]
 
 
    Tables

  [Table 1], [Table 2], [Table 3], [Table 4], [Table 5], [Table 6], [Table 7]



 

Top
Print this article  Email this article
            

    

 
   Search
 
  
    Similar in PUBMED
    Search Pubmed for
    Search in Google Scholar for
  Related articles
    Article in PDF (959 KB)
    Citation Manager
    Access Statistics
    Reader Comments
    Email Alert *
    Add to My List *
* Registration required (free)  


    Abstract
   Introduction
    Materials and Me...
   Results
   Discussion
   Conclusions
    References
    Article Figures
    Article Tables

 Article Access Statistics
    Viewed156    
    Printed4    
    Emailed0    
    PDF Downloaded45    
    Comments [Add]    

Recommend this journal

Journal of Oral and Maxillofacial Pathology | Published by Wolters Kluwer - Medknow
Online since 15th Aug, 2007